ACESO 早期懷孕檢測
K 號：K234152 · 2024-04-05
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器材摘要
ACESO Early Pregnancy Test is the device name listed in this FDA 510(k) record. The listed applicant is Aceso Laboratories, Inc.. It received FDA 510(k) clearance on 2024-04-05 under 510(k) number K234152. The device is classified under product code LCX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ACESO Early Pregnancy Test?
ACESO Early Pregnancy Test is a medical device that received FDA 510(k) clearance on 2024-04-05. The listed applicant is Aceso Laboratories, Inc.. The 510(k) number is K234152.
When did ACESO Early Pregnancy Test receive FDA 510(k) clearance?
ACESO Early Pregnancy Test received FDA 510(k) clearance on 2024-04-05, under 510(k) number K234152.
Who is the listed applicant for ACESO Early Pregnancy Test?
The FDA 510(k) record lists Aceso Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ACESO Early Pregnancy Test?
The FDA product code for ACESO Early Pregnancy Test is LCX.
相關臨床試驗
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相關器械（代碼：LCX）
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
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官方來源
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